From diagnostics and result reporting to therapy recommendations
The need for endocrinological testing arises in various fields of healthcare: in general practice, in paediatric, dermatological and very commonly in internal medicine practice, and in gynaecological or urological hormone consultation. Limbach Gruppe’s laboratory medicine specialists support physicians with a full range of laboratory diagnostic services and assessments contributed by endocrinological clinicians in the respective specialist area, including concrete practical therapy recommendations.
Paediatric endocrinology, e.g. growth disorders, adrenal gland disorders, disorders of pubertal development, obesity, diabetes mellitus
Internal endocrinology, e.g. thyroid disorders, bone metabolism, andrology, pituitary disorders, diagnostic assessment of endocrine hypertension
Our core services in molecular endocrinology
Human genetic testing for diagnostic assessment of hereditary endocrine disorders. This includes congenital adrenal hyperplasia, familial hyperaldosteronism, multiple endocrine neoplasia, MODY diabetes, neonatal diabetes mellitus, apparent mineralocorticoid excess, glucocorticoid remediable aldosteronism, pseudohyperparathyroidism, thyroid hormone resistance, acromegaly and pituitary adenomas.
Human genetic testing for diagnostic assessment of hereditary disorders of the calcium/phosphate balance, lipid metabolism and iron metabolism. The current Molecular Endocrinology Request Form is available for download here.
The German Genetic Diagnostics Act (Gendiagnostikgesetz, GenDG) requires the provision of detailed information on the nature, significance and scope of the test, as well as written patient consent (informed consent) before conducting any diagnostic or predictive genetic tests.
Dr. med. Jens KöhlerSpecialist in internal medicine and hematology and oncology
Laboratory of Molecular Endocrinology
+49 6221 658 883